A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153930



Internal ID15881273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:51981695..52093054hg38UCSC Ensembl
Innerchr5:51277529..51388888hg19UCSC Ensembl
Innerchr5:51313286..51424645hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38111360
hg19111360
hg18111360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598148
Supporting Variants
SamplesNINDS_94
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153930
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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